Job Description Wil jij met jouw expertise bijdragen aan een gezondere wereld? Binnen ons innovatieve team in Haarlem zorg je samen met collega’s voor de veilige distributie van geneesmiddelen en vaccins naar meer dan 140 landen.
At Gilead, we’re creating a healthier world for all people. For more than 35 years, we’ve tackled diseases such as HIV, viral hepatitis, COVID-19 and cancer – working relentlessly to develop therapies that help improve lives
About the Job As Senior Clinical Lead, Early Clinical & Experimental Therapeutics within our Translational Medicine Unit, youll be at the forefront of oncology drug development—designing and leading early clinical studies that could transform treatment options
Our mission LOGEX is at the forefront of healthcare analytics in Europe, transforming data into actionable insights to address the complex challenge of managing costs while improving clinical outcomes. Headquartered in Amsterdam, LOGEX boasts an international
Are you passionate about healthcare innovation and curious about how new ideas become real-world improvements for patients and healthcare professionals? The Clinical Study Unit (CSU) part of Sanofis North Europe MCO, is looking for a Local
Job grade: FGIV Internal/inter-agency job grade: FGIV Type of position: Contract agent Selection procedure reference: EMA/CA/11523 Job title: Transparency Officer Talent Pool: FGIV Science and Regulation Deadline for applications: 06 September 2026 at 23:59 CEST Salary: 4249,97
Were looking for 2 organized and detail-oriented Assistants to join our Regulatory Affairs HUB Netherlands in Alkmaar. This is an excellent opportunity for someone early in their career who is eager to learn regulatory processes and
Company Description Santen is a specialized life sciences company with a proud over 130-year heritage focused exclusively on ophthalmology. As a Japan-originated, global company with a footprint in over 60 countries, we are dedicated to delivering innovative
Join EVA Pharma, a leading pharmaceutical company dedicated to empowering the fight for health and well-being as a fundamental human right. Recognized and certified as a best place to work, we are committed to fostering a supportive
Associate Consultant and Statistician, Statistics & Psychometrics – Patient Centered Solutions Overview IQVIA provides scientific services spanning clinical trials, real world evidence, and consulting in all areas of the product lifecycle. The Patient Centered Solutions (PCS)
Clinical Trial Psych Rater - Dutch Speaking Location: Remote/Virtual Hours: Estimated 10–16 hours per month Role: Clinical Specialist About IQVIA IQVIA is a global leader in advanced analytics, technology solutions, and clinical research services, dedicated to
Job Description Shape the future with data! We are building a truly insight-driven organization where data and AI power smarter decisions across the business. Join our team to turn complex data into meaningful insights and help
Lead Data Engineer About IQVIA Patient Finder We live in a world where most information is readily available at our fingertips. You might be surprised to learn the situation in hospitals is rather different. Systems used
Job title: Market Access Associate Location: Amsterdam, Netherlands Job type: Full time, Hybrid About the job About the opportunity In this role you will contribute to, and coordinate where appropriate, activities related to the development of
Senior Consultant - 360 recruitment - Perm desk - Amsterdam The Role We are looking for a Senior Recruitment Consultant to join our permanent team. This is a true 360 recruitment role, responsible for both business
Join Us Join us as we continue to grow our presence in Medical Technology and Digital Health - two of the most innovative and fast-moving areas within Life Sciences, shaping the future of healthcare through technology and
Are you an analytical laboratory professional who would like to contribute to medicines used by patients worldwide? For an international pharmaceutical manufacturing organisation in Haarlem, we are looking for an Analyst I to join a GMP-regulated Quality
Avertim Netherlands is currently looking for Process Engineers able to assist in the continuous expansion of Avertim’s consulting activities in Life Sciences & Chemicals. Located in Amsterdam-Zuid, Avertim Netherlands is a trusted partner of the largest players
As our Validation Specialist IT (CSV/CSA), you will lead validation and compliance activities for GxP-regulated systems, digital transformation initiatives, equipment, infrastructure, and system integration projects across Prothya. Your role is responsible for defining validation strategies, ensuring
Are you detail-oriented and organized Administrative Assistant to support our Quality Control (QC) department with documentation management, archiving, training administration, and laboratory support activities? Key Responsibilities: Documentation & Archiving Review, bind, and archive QC worklists Manage